Pierre Billuart
Pierre Billuart
在 inserm.fr 的电子邮件经过验证 - 首页
Somatic mutations of the β-catenin gene are frequent in mouse and human hepatocellular carcinomas
A de La Coste, B Romagnolo, P Billuart, CA Renard, MA Buendia, ...
Proceedings of the National Academy of Sciences 95 (15), 8847-8851, 1998
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome
V des Portes, JM Pinard, P Billuart, MC Vinet, A Koulakoff, A Carrié, ...
Cell 92 (1), 51-61, 1998
Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation
P Billuart, T Bienvenu, N Ronce, V Des Portes, MC Vinet, R Zemni, ...
Nature 392 (6679), 923-926, 1998
A new gene involved in X-linked mental retardation identified by analysis of an X; 2 balanced translocation
R Zemni, T Bienvenu, MC Vinet, A Sefiani, A Carrié, P Billuart, ...
Nature genetics 24 (2), 167-170, 2000
Regulating axon branch stability: the role of p190 RhoGAP in repressing a retraction signaling pathway
P Billuart, CG Winter, A Maresh, X Zhao, L Luo
Cell 107 (2), 195-207, 2001
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes
H Hu, SA Haas, J Chelly, H Van Esch, M Raynaud, APM De Brouwer, ...
Molecular psychiatry 21 (1), 133-148, 2016
Loss of X-linked mental retardation gene oligophrenin1 in mice impairs spatial memory and leads to ventricular enlargement and dendritic spine immaturity
M Khelfaoui, C Denis, E Van Galen, F De Bock, A Schmitt, C Houbron, ...
Journal of Neuroscience 27 (35), 9439-9450, 2007
The RhoGAP activity of OPHN1, a new F-actin-binding protein, is negatively controlled by its amino-terminal domain
F Fauchereau, U Herbrand, P Chafey, A Eberth, A Koulakoff, MC Vinet, ...
Molecular and Cellular Neuroscience 23 (4), 574-586, 2003
A mosaic genetic screen for genes necessary for Drosophila mushroom body neuronal morphogenesis
JE Reuter, TM Nardine, A Penton, P Billuart, EK Scott, T Usui, T Uemura, ...
Development 130 (6), 1203-1213, 2003
Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia
G Zanni, Y Saillour, M Nagara, P Billuart, L Castelnau, C Moraine, ...
Neurology 65 (9), 1364-1369, 2005
A postsynaptic signaling pathway that may account for the cognitive defect due to IL1RAPL1 mutation
A Pavlowsky, A Gianfelice, M Pallotto, A Zanchi, H Vara, M Khelfaoui, ...
Current Biology 20 (2), 103-115, 2010
Inhibition of RhoA pathway rescues the endocytosis defects in Oligophrenin1 mouse model of mental retardation
M Khelfaoui, A Pavlowsky, AD Powell, P Valnegri, KW Cheong, Y Blandin, ...
Human molecular genetics 18 (14), 2575-2583, 2009
Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitor
T Bienvenu, V Des Portes, A Saint Martin, N McDonell, P Billuart, A Carrié, ...
Human molecular genetics 7 (8), 1311-1315, 1998
Doublecortin interacts with μ subunits of clathrin adaptor complexes in the developing nervous system
G Friocourt, P Chafey, P Billuart, A Koulakoff, MC Vinet, BT Schaar, ...
Molecular and Cellular Neuroscience 18 (3), 307-319, 2001
Emerging major synaptic signaling pathways involved in intellectual disability
A Pavlowsky, J Chelly, P Billuart
Molecular psychiatry 17 (7), 682-693, 2012
Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22.
V Des Portes, JM Pinard, D Smadja, J Motte, O Boespflüg-Tanguy, ...
Journal of medical genetics 34 (3), 177-183, 1997
A circadian clock in hippocampus is regulated by interaction between oligophrenin-1 and Rev-erbα
P Valnegri, M Khelfaoui, O Dorseuil, S Bassani, C Lagneaux, A Gianfelice, ...
Nature neuroscience 14 (10), 1293-1301, 2011
Autophosphorylation-independent and-dependent functions of focal adhesion kinase during development
JM Corsi, C Houbron, P Billuart, I Brunet, K Bouvrée, A Eichmann, ...
Journal of Biological Chemistry 284 (50), 34769-34776, 2009
Mapping of the X-breakpoint involved in a balanced X; 12 translocation in a female with mild mental retardation
T Bienvenu, H Der-Sarkissian, P Billuart, M Tissot, V Des Portes, T Brüls, ...
European Journal of Human Genetics 5, 105-109, 1997
Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes
C Delépine, H Meziane, J Nectoux, M Opitz, AB Smith, C Ballatore, ...
Human molecular genetics 25 (1), 146-157, 2016
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